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Hierarchical recruitment of Polycomb complexes revisited

Polycomb Group (PcG) proteins epigenetically repress key developmental genes and thereby control alternative cell fates. PcG proteins act as complexes that can modify histones and these histone modifications play a role in transmitting the “memory” of the repressed state as cells divide. Here we con...

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Autores principales: Dorafshan, Eshagh, Kahn, Tatyana G., Schwartz, Yuri B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703234/
https://www.ncbi.nlm.nih.gov/pubmed/28910569
http://dx.doi.org/10.1080/19491034.2017.1363136
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author Dorafshan, Eshagh
Kahn, Tatyana G.
Schwartz, Yuri B.
author_facet Dorafshan, Eshagh
Kahn, Tatyana G.
Schwartz, Yuri B.
author_sort Dorafshan, Eshagh
collection PubMed
description Polycomb Group (PcG) proteins epigenetically repress key developmental genes and thereby control alternative cell fates. PcG proteins act as complexes that can modify histones and these histone modifications play a role in transmitting the “memory” of the repressed state as cells divide. Here we consider mainstream models that link histone modifications to hierarchical recruitment of PcG complexes and compare them to results of a direct test of interdependence between PcG complexes for recruitment to Drosophila genes. The direct test indicates that PcG complexes do not rely on histone modifications to recognize their target genes but use them to stabilize the interactions within large chromatin domains. It also shows that multiple strategies are used to coordinate the targeting of PcG complexes to different genes, which may make the repression of these genes more or less robust.
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spelling pubmed-57032342017-12-01 Hierarchical recruitment of Polycomb complexes revisited Dorafshan, Eshagh Kahn, Tatyana G. Schwartz, Yuri B. Nucleus Extra View Polycomb Group (PcG) proteins epigenetically repress key developmental genes and thereby control alternative cell fates. PcG proteins act as complexes that can modify histones and these histone modifications play a role in transmitting the “memory” of the repressed state as cells divide. Here we consider mainstream models that link histone modifications to hierarchical recruitment of PcG complexes and compare them to results of a direct test of interdependence between PcG complexes for recruitment to Drosophila genes. The direct test indicates that PcG complexes do not rely on histone modifications to recognize their target genes but use them to stabilize the interactions within large chromatin domains. It also shows that multiple strategies are used to coordinate the targeting of PcG complexes to different genes, which may make the repression of these genes more or less robust. Taylor & Francis 2017-09-14 /pmc/articles/PMC5703234/ /pubmed/28910569 http://dx.doi.org/10.1080/19491034.2017.1363136 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Extra View
Dorafshan, Eshagh
Kahn, Tatyana G.
Schwartz, Yuri B.
Hierarchical recruitment of Polycomb complexes revisited
title Hierarchical recruitment of Polycomb complexes revisited
title_full Hierarchical recruitment of Polycomb complexes revisited
title_fullStr Hierarchical recruitment of Polycomb complexes revisited
title_full_unstemmed Hierarchical recruitment of Polycomb complexes revisited
title_short Hierarchical recruitment of Polycomb complexes revisited
title_sort hierarchical recruitment of polycomb complexes revisited
topic Extra View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703234/
https://www.ncbi.nlm.nih.gov/pubmed/28910569
http://dx.doi.org/10.1080/19491034.2017.1363136
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